Thermoplastic pavement marking composition and method

ABSTRACT

A composition of matter suitable for use as a road marking substance and a method thereof provides for the steps of mixing a binder mixture with a filler mixture, heating the mixed ingredients while mixing into a homogenous molten mixture and then extruding the molten mixture. The extruded material is cooled, cut into individual pellets, coated with an anti-clumping coating and packaged for use in making a road marking substance in situ. The binder can be alkyd-based or hydrocarbon based. The binder includes rosin resins, wax and a plasticizer, and a hydrocarbon resin is added for the hydrocarbon-based binder. The filler contains titanium dioxide, a pigment (if necessary) and ground calcium carbonate.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of my co-pending applicationSer. No. 14/329,462 filed on Jul. 11, 2014, entitled “Pelletizing systemfor thermoplastic pavement marking material,” which is acontinuation-in-part of my co-pending application Ser. No. 14/270,068filed on May 5, 2014 entitled “Pelletizing system for road surfacemarking material,” the full disclosures of which are incorporated byreference herein and priority of which is hereby claimed.

BACKGROUND OF THE INVENTION

Road surface markings are used on paved roadways to provide guidance andinformation to drivers and pedestrians. Road surface markings can beformed using mechanical or non-mechanical devices. Mechanical roadsurface markers may be raised or recessed into the road surface, and canbe either reflective or non-reflective. Examples of mechanical markersare Botts' dots and rumble strips. Non-mechanical markers may be formedby paint, thermoplastic, preformed polymer tape, epoxy and othermethods.

Thermoplastic markers are some of the most common types of road markingbased on their balance between cost and performance longevity.Thermoplastic binder systems are generally based on one of three corechemistries: hydrocarbons, rosin esters, and maleic modified rosinesters (MMRE). Thermoplastic coatings are generally homogeneous drymixes of binder resins, plasticizers, glass beads (or other optics),pigments, and fillers. These types of markers demonstrate increaseddurability, lasting 3 to 6 years, and retro-reflectivity.

Thermoplastic pavement markings are used in a hot-melt applicationprocess for various types of traffic control indicia. They are normallycomprised of alkyd or hydrocarbon based resin systems, although hybridversions of the materials can be formulated to impart favorableproperties of each individual system into one combined system.Typically, thermoplastic pavement marking materials are used on roadwaysin longitudinal lines as edge and center-lines either as a continuousline or a skipped/dashed line. They can also be used for transversemarkings such as stop bars, chevrons, traffic taming markings, bike andpedestrian crossings, railroad crossings, or similar markings.Thermoplastic pavement markings are used on public and private highways,public and private properties, airports, and parking lots.

Thermoplastic pavement are non-reactive coatings systems that are 100%solids materials composed of binder, pigment, glass beads, and inertfillers. Each state, and some cities and counties, govern the type andapplication of thermoplastic application by specifying the chemicalcomposition and final film properties in terms of field performance overthe lifecycle of the marking. Although most governmental agencies havetheir own internal and independent pavement marking specifications,thermoplastic pavement marking specifications are normally based on somevariation of AASHTO M-249, which is a federal specification that setsminimum and basic requirements of the materials to be used. The binderis made up of a combination of rosin or petroleum based resins,plasticizing oils, elastomers, and viscosity and flow modifiers. Thepigment for white materials is predominately Type II rutile titaniumdioxide. The pigment for yellow materials is an organic based yellowpigment which can be a combination of yellow and red or orange pigmentsdesigned to withstand high temperatures and provide excellent UVresistance and weatherability. Glass beads are incorporated into thematerial so that as the material degrades under UV, water, and trafficexposure the glass beads will become exposed and serve as reflectiveelements for nighttime visibility while under illumination fromvehicles' headlamps. An exemplary compositional range for each componentis as follows: binder 18-26%, pigment (TiO2 only) 10-12% for white, N/Afor yellow, and beads 30-40%.

Conventional thermoplastic mix is supplied in powdered form, which makesit difficult to load into the road marking machine. The technicians haveto strictly follow safety regulations and use special equipment whenpreparing the marking mix. My co-pending application Ser. No. 14/329,462filed on Jul. 11, 2014 discloses a system of producing pelletizedthermoplastic pavement marking material, which eliminates orsignificantly minimizes hazards associated with dust produced bypowdered mixes. This application is directed to an apparatus and methodof producing the thermoplastic pavement marking material in a pelletizedform.

SUMMARY OF THE INVENTION

It is, therefore, an object of the present invention to provide anapparatus and method of making a pelletizing material that can be usedfor creating thermoplastic pavement markers.

It is another object of the invention to provide a pelletizing systemcapable of pelletizing a mixture of raw materials with embeddedreflective elements.

It is a further object of the invention to provide a composition andmethod of producing pelletized road marking material, while mixing thepowdered materials with reflective elements.

These and other objects of the invention are achieved through aprovision of a composition of matter suitable for use as a road markingsubstance and a method thereof provides for the steps of mixing a bindermixture with a filler mixture, heating the mixed ingredients whilemixing into a homogenous molten mixture and then extruding the moltenmixture. The extruded material is cooled, cut into individual pellets,coated with an anti-clumping coating and packaged for use in making aroad marking substance in situ. The binder can be alkyd-based orhydrocarbon based. The binder includes rosin resins, wax and aplasticizer, and a hydrocarbon resin is added for the hydrocarbon-basedbinder. The filler contains titanium dioxide, a pigment (if necessary)and ground calcium carbonate.

BRIEF DESCRIPTION OF THE DRAWINGS

Reference will now be made to the drawings, wherein like parts aredesignated by like numerals, and wherein

FIG. 1 is a schematic view of the pelletizing system of the presentinvention.

DETAIL DESCRIPTION OF THE INVENTION

Turning now to the drawing in more detail, numeral 10 designates thepelletizing system of the present invention. The system 10 includes amixing station 12, a cooling station 14, a drying station 16, and apellet-coating station 18.

The mixing station 12 comprises a plurality of separate containers 22,each of which is configured to retain a pre-determined quantity ofstarting raw material, from which the pellets for the pavement markingare manufactured. The containers 22 are made as hoppers with open topsallowing the operators to deposit the raw materials therein. Rawmaterials are maintained in the storage hoppers 22 and gravity fed to aweight load cell 26, which accurately delivers raw materials in thedesired weight proportion. In the exemplary embodiment of FIG. 1, eachcontainer or storage hopper 22 is provided with an individual loss inweight load cell 26. However that number can vary up or down dependingon the number of components needed for the desired end product. The rawmaterials can be added in a liquid, solid, powder, or paste form; resinscan be bought in liquid bulk containers eliminating paper, plastic, andpallet packaging.

In general, thermoplastic pavement marking materials are designed toimpart compositional and physical properties outlined in FederalSpecification AASHTO M249, but the material formulation can be modifiedto meet any applicable governmental agencies material requirements.AASHTO T250 test methods are used to determine material composition andphysical characteristics.

Thermoplastic materials are typically based on hydrocarbon or alkydresins. Materials produced using hydrocarbon based resins are used inlong-line or longitudinal applications, whereas alkyd formulations canbe used in any application. The alkyd-based composition of thethermoplastic marking material of the instant invention comprises abinder, pigment, glass beads, and fillers.

Alkyd based thermoplastic binders are comprised of a combination of oneor more member selected from the group consisting of rosin resins,waxes, and plasticizers. More specifically, the rosin resin is comprisedof one or more member of the group consisting of modified rosin resinsand rosin esters. Modified rosin resins are comprised of one or morecomponent of the group consisting of rosin acids, maleic anhydride, andfumaric acid. Rosin acids, derived from pine trees as gum rosin, woodrosin, or tall oil rosin, are comprised of one or more component of thegroup consisting of abeitic acid, neoabeitic acid, dehydroabeitic acid,levopimaric acid, pimaric acid, palustric acid, isopimaric acid, andsandarocopimaric acid. Rosin esters are comprised of one or morederivative obtained from the reaction of one or more rosin acids and oneor more alcohol from the group of alcohols consisting of methanol,triethylene glycol, glycerol, and pentaerythritol.

The waxes are comprised of one or more member selected from the groupconsisting of vegetable waxes, petroleum derived waxes, and syntheticwaxes. Vegetable waxes used in thermoplastics are normally naturallyoccurring mixtures of long-chain aliphatic hydrocarbons, containingesters of fatty acids and alcohols. The fatty acids are comprised of oneor more component of the group consisting of ricinoleic acid, oleicacid, linoleic acid, linolenic acid, stearic acid, palmitic acid,dihydroxy stearic acid, myristic acid, myristoleic acid, palmitoleicacid, sapeinic acid, elaidic acid, vaccenic acid, alpha-linolenic acid,arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoicacid, caprylic acid, capric acid, lauric acid, arachidic acid, behenicacid, lignoceric acid, and cerotic acid.

The alcohols are comprised of one or more members selected from thegroup consisting of glycerol, ethanol, methanol, pentaerythritol,iso-propanol, isopropyl alcohol, butanol, dihydroxy butanol, or anyother mono-functional or multi-functional alcohol a varying long-chainaliphatic hydrocarbon backbone.

Petroleum derived waxes are comprised of one or more member selectedfrom the group consisting of saturated n-alkanes, iso-alkanes,napthenes, alkyl-substituted aromatic compounds, andnapthene-substituted aromatic compounds. Synthetic waxes can bepolyethylene, Fischer-Tropsch waxes, chemically modified waxes, or amidemodified waxes. Polyethylene waxes generally have the chemical formula(C2H4)nH2 and are comprised, based on branching and chemical structure,of one or more component of the group consisting ofultra-high-molecular-weight polyethylene (UHMWPE), high-densitypolyethylene (HDPE), cross-linked polyethylene (PEX or XLPE),medium-density polyethylene (MDPE), linear low-density polyethylene(LLDPE), low-density polyethylene (LDPE), very-low-density polyethylene(VLDPE), and copolymers. Fischer-Tropsch waxes generally have thechemical formula (CnH(2n+2)).

Chemically modified waxes are converted from non-polar to polarmolecules by the incorporation of a functional chemical group comprisedof one or more component consisting of a hydroxyl group, a carboxylgroup, a salt, an ester group, and an acid group. Amide modified waxesare chemically modified waxes that have amide functional moleculesgrafted to the polyethylene molecule to modify flexibility, adhesion, orsystem compatibility of the wax.

Plasticizers are comprised of one or more member selected from the groupconsisting of vegetable oils, synthetic alkyd oils, and phthalates.Vegetable oils, called triglycerides because they are the resultantreaction of fatty acids with glycerol, and synthetic alkyd oils are madeof fatty acid esters of varying composition. The fatty acids found intheir structure are comprised of one or more components of the groupconsisting of ricinoleic acid, oleic acid, linoleic acid, linolenicacid, stearic acid, palmitic acid, dihydroxy stearic acid, myristicacid, myristoleic acid, palmitoleic acid, sapeinic acid, elaidic acid,vaccenic acid, alpha-linolenic acid, arachidonic acid, eicosapentaenoicacid, erucic acid, docosahexaenoic acid, caprylic acid, capric acid,lauric acid, arachidic acid, behenic acid, lignoceric acid, and ceroticacid. Phthalates are comprised of one or more components from the groupconsisting of dimethyl phthalate, diethyl phthalate, diallyl phthalate,di-n-propyl phthalate, di-n-butyl phthalate, diisobutyl phthalate, butylcyclohexyl phthalate, di-n-pentyl phthalate, dicyclohexyl phthalate,butyl benzyl phthalate, di-n-hexyl phthalate, diisohexyl phthalate,diisoheptyl phthalate, butyl decyl phthalate, butyl(2-ethylhexyl)phthalate, di(n-octyl) phthalate, diisooctyl phthalate, n-octyl n-decylphthalate, diisononly phthalate, di(2-prpoylheptyl) phthalate,diisodecyl phthalate, diundecyl phthalate, diisoundecyl phthalate,ditridecyl phthalate, and diisotridecyl phthalate.

The hydrocarbon based thermoplastic binder is comprised of one or morecomponents selected from the group consisting of hydrocarbon resins,rosin resins, waxes, and plasticizers. The hydrocarbon resin iscomprised of one or more component selected from the group consisting ofC5 aliphatic hydrocarbon resins, C9 aromatic hydrocarbon resins, andC5/C9 hydrocarbon blend. C5 aliphatic hydrocarbon resins are producedfrom the distillation reaction, in the presence of a Lewis catalyst, ofpiperylene which is comprised of one or more components of the groupconsisting of trans-1,3-pentadiene, cis-1,3- pentadiene,2-methyl-2-butene, dicyclopentadiene, cyclopentadiene, and cyclopentene.

C9 aromatic hydrocarbon resins are a byproduct of the naptha cracking ofpetroleum feedstocks used to produce C5 aliphatic resins and arecomprised of one or more components of the group consisting ofvinyltoluenes, dicyclopentadiene, indene, methylstyrene, styrene, andmethylindenes.

The rosin resin is comprised of one or more component selected from thegroup consisting of modified rosin resins and rosin esters. Modifiedrosin resins are comprised of one or more component selected from thegroup consisting of rosin acids, maleic anhydride, and fumaric acid.Rosin acids, derived from pine trees as gum rosin, wood rosin, or talloil rosin, are comprised of one or more component of the groupconsisting of abeitic acid, neoabeitic acid, dehydroabeitic acid,levopimaric acid, pimaric acid, palustric acid, isopimaric acid, andsandarocopimaric acid. Rosin esters are comprised of one or morederivative obtained from the reaction of one or more rosin acids and oneor more alcohol from the group of alcohols consisting of methanol,triethylene glycol, glycerol, and pentaerythritol.

The waxes used in the hydrocarbon based binder system are comprised ofone or more components selected from the group consisting of petroleumwaxes or synthetic waxes. Petroleum derived waxes are comprised of oneor more member selected from the group consisting of saturatedn-alkanes, iso-alkanes, napthenes, alkyl-substituted aromatic compounds,and napthene-substituted aromatic compounds. Synthetic waxes can bepolyethylene, Fischer-Tropsch waxes, chemically modified waxes, or amidemodified waxes.

Polyethylene waxes generally have the chemical formula (C2H4)nH2 and arecomprised, based on branching and chemical structure, of one or morecomponent of the group consisting of ultra-high-molecular-weightpolyethylene (UHMWPE), high-density polyethylene (HDPE), cross-linkedpolyethylene (PEX or XLPE), medium-density polyethylene (MDPE), linearlow-density polyethylene (LLDPE), low-density polyethylene (LDPE),very-low-density polyethylene (VLDPE), and copolymers. Fischer-Tropschwaxes generally have the chemical formula (CnH(2n+2)).

Chemically modified waxes are converted from non-polar to polarmolecules by the incorporation of a functional chemical group comprisedof one or more component consisting of a hydroxyl group, a carboxylgroup, a salt, an ester group, and an acid group. Amide modified waxesare chemically modified waxes that have amide functional moleculesgrafted to the polyethylene molecule to modify flexibility, adhesion, orsystem compatibility of the wax.

The plasticizers used in the hydrocarbon binder system are comprised ofone or more member selected from the group consisting of process oilsand phthalates. Process oils are comprised of one or more components ofthe group consisting of paraffinic oils, napthenic oils, and aromaticoils. All of the process oils are derived from the petroleum refiningindustry as distillates and are separated based on degree ofcarbon-carbon saturation.

Paraffinic oils are saturated carbon backbones, napthenic oils havepolyunsaturated carbon structure with little aromatic content, andaromatic oils have cyclic carbon unsaturation resulting aromaticclassification. Phthalates are comprised of one or more components fromthe group consisting of dimethyl phthalate, diethyl phthalate, diallylphthalate, di-n-propyl phthalate, di-n-butyl phthalate, diisobutylphthalate, butyl cyclohexyl phthalate, di-n-pentyl phthalate,dicyclohexyl phthalate, butyl benzyl phthalate, di-n-hexyl phthalate,diisohexyl phthalate, diisoheptyl phthalate, butyl decyl phthalate,butyl(2-ethylhexyl) phthalate, di(n-octyl) phthalate, diisooctylphthalate, n-octyl n-decyl phthalate, diisononly phthalate,di(2-prpoylheptyl) phthalate, diisodecyl phthalate, diundecyl phthalate,diisoundecyl phthalate, ditridecyl phthalate, and diisotridecylphthalate.

The pigment can be Rutile Type II titanium dioxide with a minimum purityof 92% for white materials and a combination of titanium dioxide andorganic or other heavy metals free yellow pigments for yellow materials.The fillers are ground calcium carbonate of various particle size basedon desired flow characteristics. The glass beads used shall be the size,quality, and concentration specified by the applicable governmentalrequirement.

In one the preferred embodiments, the alkyd binder comprises a mixtureof maleic modified glycerol ester and pentaerythritol ester of rosinresins, high density polyethylene or other acid or amine functional highdensity polyethylene waxes, low density copolymer of polyethylenethermoplastic elastomers, and synthetic or natural, solid or liquidplasticizers based soya, castor, or palm chemistries.

The hydrocarbon binder prepared according to the instant inventioncomprises a blend of petroleum based C-5 resins (tackifiers),pentaerythritol or maleic modified ester of rosin resin, low densitypolyethylene wax/elastomer, an acid or amine functional based lowdensity polyethylene, high density polyethylene waxes (HDPE), and aparaffinic, naphthenic oil used as a liquid plasticizer. The pigmentused in the road marking composition of this invention can be RutileType II titanium dioxide with a minimum purity of 92% for whitematerials and a combination of titanium dioxide and organic or otherheavy metals free yellow pigments for yellow materials. The fillers usedin the composition of the instant invention are ground calcium carbonateof various particle size based on desired flow characteristics. Theglass beads used in the instant composition depend on the applicablegovernmental requirement for the size, quality, and concentration.

In the preferred embodiments, white alkyd-based binder mixture containsbetween 8% and 16% by weight of rosin resin with a melt point of between95° and 110° C., between 0.01% and 3% by weight of wax with a meltingpoint of between 95° and 115° C., and a non-drying polar materialplasticizer in the amount of between 0.01% and 3% by weight. The totalbinder mixture present in the road marking composition is between 18%and 26% by weight.

EXAMPLE 1

One specific example of a white alkyd-based binder mixture contains13.6% by weight of a rosin resin, 2.5% by weight of wax, and 1.9% byweight of a plasticizer. Total binder weight is 19%.

In the preferred embodiments, white filler mixture for alkyd-basedbinder contains titanium dioxide (Rutile Type II) of 92% minimum purityin the amount of between 10% and 12% by weight, AASHTO Type I GlassBeads 70% Rounds Minimum in the amount of between 30% and 40% by weight,and Ground Calcium Carbonate +/−325 Mesh in the amount of between 34%and 42% by weight.

EXAMPLE 1-1

In one specific example, the white filler mixture for the alkyd-basedcomposition comprises about 10% by weight of titanium dioxide, about 30%by weight of AASHTO Type I Glass Beads, and about 41% of calciumcarbonate. The softening point of the binder and the filler, in thepreferred embodiment, is about 104.44° C.

In the preferred embodiments, yellow-tinted alkyd-based binder mixturecontains the same ingredients as the white alkyd-based binder. However,the pigment mixture is different. The filler mixture for a yellow-tintedalkyd-based binder contains titanium dioxide in the amount of between0.5% and 3% by weight, AASHTO Type I Glass Beads 70% Rounds Minimum inthe amount of between 30% and 40% by weight, organic or lead-free yellowpigment in the amount of between 0.25% and 1.25% by weight, organic orlead-free heat-resistant orange in the amount of 0.05% to 0.25% byweight, and a sufficient amount of Ground Calcium Carbonate +/−325 Meshto constitute 100% of the road marking composition. The softening pointof the binder and the filler, in the preferred embodiment, is about104.44° C.

EXAMPLE 1-2

In one example, the yellow filler mixture for alkyd-based bindercontains 1.5% by weight of titanium dioxide, about 0.5% by weight ofOrganic Yellow 83 pigment, 0.05% by weight of lead-free orange pigment,about 30% by weight of AASHTO Type I Glass Beads 70% Rounds Minimum, andabout 49% by weight of ground calcium carbonate.

In an exemplary embodiment of the composition of the thermoplastic roadmarking material prepared according to the method of the presentinvention, the alkyd-based binder comprises maleic modified alkyd resinin the amount of between 8% and 16% by weight, pentaerythritol (PE)alkyd resin in the amount of between 0.01% and 7% by weight, highdensity polyethylene (HDPE) or similar wax in the amount of between0.01% and 3%, an elastomer in the amount of between 0.25% and 3%, and aplasticizer in the amount of between 0.01% and 3%. The plasticizer canbe liquid, solid, or paste.

In the preferred embodiments of the alkyd-base binder, maleic modifiedalkyd resin has a melting point of between 95° and 110° C.,pentaerythritol (PE) alkyd resin has a melting point of between 95° and110° C., high density polyethylene (HDPE) or similar wax has a meltingpoint of between 95° and 115° C., elastomer has a melt flow index ofbetween 0 and 1000, and the plasticizer is a non-drying polar material.

EXAMPLE 1-3

In one specific example, the alkyd-based binder mixture comprises 13.6%by weight of maleic modified alkyd resin, 2.5% by weight of high densitypolyethylene, 1% by weight of elastomer and 1.9% by weight of aplasticizer. Pentaerythritol (PE) alkyd resin is an optional ingredientin this particular example.

The binder mixture is present in the finished composition in the amountof between 18% and 26% by weight. In the specific example above, thebinder total is about 19% by weight. To the binder mixture, a fillermixture is added to make up 100% by weight of the road markingmaterials.

The present invention further contemplates provision of ahydrocarbon-based road marking composition. In such compositions, thepetroleum-based binder comprises between 10 and 15% by weight of ahydrocarbon resin with a melt point of between 95° and 110° C., between0.01% and 3% by weight of rosin resin with a melt point of 95° and 110°C., between 0.01% and 3% of a wax with a melt point of 95° and 115° C.,and between 0.01% and 2% by weight of a plasticizer, such as White Oilor similar substance. The total binder present in the finishedpetroleum-based road marking composition is between 18% and 26% byweight. White filler mixture for the petroleum-based binder is similarto the white filler mixture for the alkyd-based binder mixture.

EXAMPLE 2

One exemplary embodiment of a petroleum-based binder contains about10.3% of a hydrocarbon resin, about 2.5% by weight of a rosin resin,about 2.5% by weight of a wax, and about 1.2% by weight of aplasticizer, with a total weight of the binder being about 19% of thetotal composition.

In the preferred embodiments, the hydrocarbon based binder mixturecontains a petroleum-based resin, such as for instance C-5 or C-9 resinin the amount of between 10% and 15% by weight, pentaerythritol (PE)alkyd resin in the amount of between 0.01% and 3% by weight, highdensity polyethylene (HDPE) or similar wax in the amount of between0.01% and 3% by weight, low density polyethylene (LDPE) in the amount ofbetween 0.01% and 3% by weight, functionalized low-density polyethylenein the amount of between 0.01% and 0.25% by weight, and a plasticizingoil (white oil or similar agent) in the amount of between 0.01% and 2%by weight. The total amount of binder in the exemplary petroleum-basedcompositions is between 18% and 26% by weight.

In the preferred embodiments of the hydrocarbon-based binder, C-5 resinhas a melting point of between 95° and 110° C., pentaerythritol (PE)alkyd resin has the melting point of between 95° and 110° C., highdensity polyethylene (HDPE) or similar wax has the melting point ofbetween 95° and 115° C., low-density polyethylene and functionalizedLDPE each have a melt flow index of between 0 and 1000, functionalizedLDPE has a melt and the plasticizing oil is a non-drying polar material.

EXAMPLE 2-1

In one specific example of the petroleum-based binder mixture, thecomposition has 10.3% by weight of C-5 resin, 2.5% by weight of PE alkydresin, 2.5% by weight of HDPE, 2.5% by weight of LDPE, and 1.2% byweight of white Oil. Functionalized LDPE is an optional ingredient inthis particular example. The binder is present in this specific examplein the amount of 19% by weight.

EXAMPLE 2-2

In another example of a petroleum-based binder mixture, the compositionhas 11.3% by weight of C-5 resin, 2.5% by weight of PE alkyd resin, 2.5%by weight of HDPE, 2.5% by weight of LDPE, and 1.2% by weight of whiteOil. Functionalized LDPE is an optional ingredient in this particularexample. The binder is present in this specific example in the amount of20% by weight.

The white tinting filler mixture for the petroleum-based binder issimilar to the filler mixture of the alkyd base composition inasmuch asit uses titanium dioxide, glass beads and calcium carbonate. In thepreferred embodiments, the white filler mixture for thehydrocarbon-based binder contains titanium dioxide (Rutile Type II) of92% minimum purity in the amount of between 10% and 12% by weight,AASHTO Type I Glass Beads 70% Rounds Minimum in the amount of between30% and 40% by weight, and Ground Calcium Carbonate +/−325 Mesh in theamount of between 34% and 42% by weight. The filler mixture is added insufficient amount to the binder mixture to make up 100% of thecomposition.

EXAMPLE 2-3

In one specific example, white-tinted filler mixture for thepetroleum-based binder comprises about 10% by weight of titaniumdioxide, about 30% by weight of AASHTO Type I Glass Beads, and about 41%by weight of calcium carbonate. The softening point of the binder andthe filler, in the preferred embodiment, is about 104.44° C.

The filler mixture for a yellow-tinted hydrocarbon-based binder containstitanium dioxide in the amount of between 0.5% and 3% by weight, AASHTOType I Glass Beads 70% Rounds Minimum in the amount of between 30% and40% by weight, organic or lead-free yellow pigment in the amount ofbetween 0.25% and 1.25% by weight, organic or lead-free heat-resistantorange in the amount of 0.05% to 0.25% by weight, and a sufficientamount of Ground Calcium Carbonate +/−325 Mesh to make up 100% of theroad marking composition.

EXAMPLE 2-4

In one specific example, a yellow-tinted filler mixture for thepetroleum-based binder comprises about 1.00% by weight of titaniumdioxide, about 30% by weight of AASHTO Type I Glass Beads, 0.6% byweight of Organic Yellow 83, 0.05% by weight of Lead-free Orangepigment, and about 48.4% by weight of calcium carbonate. The softeningpoint of the binder and the filler, in the preferred embodiment, isabout 104.44° C.

Raw material components processed in the apparatus 10 in making roadmarking composition according to this invention are received in bulkpowder, bulk liquid, super sack powder, super sack flake, super sackpellet, super sack prill, bag powder, bag flake, bag pellet, or bagprill form.

The containers 22 with the raw materials are mounted on a superstructure30, below which an extruder assembly is located. Raw material from eachweight load cell 26 is dispensed, by gravity to an auger mixer assemblyor extruder assembly 32. Some of the more sensitive components of themixture of raw materials are fed into the auger mixer assembly 32downstream from an upstream intake end 34, as is schematically shown byarrows 36 in FIG. 1. In one aspect of the invention, the auger mixerassembly 32 comprises a co-rotating twin screw extruder.

All binder components except liquid plasticizers are metered into theextruder in conjunction with all titanium dioxide and ½ of the filler asthe extruder screw(s) rotate and propagate material flow down theextruder barrel 40. The screw extruders or augers 42 mix the componentsinto a homogenous mixture, which is transported along the extruderbarrel 40, within which the auger 42 rotates.

The extruder's barrel 40 is heated by friction and/or with electricheater bands 46 or cooled with pumped water (via a water jacketedbarrel) as desired or required by the material being produced. The firstsection of the extruder (the feed section) 34 is used to feed theinitial components into the mixing and kneading section of the screw 42where the rest of the filler and glass beads and any liquid plasticizersare introduced according to the formulation's required rate. The initialcomponents are melted into a liquid form at a temperature of 137.78° C.at the point of union with the secondary raw material addition. Allmaterials are blended and heated further in the mixing and kneadingsection of the auger 42 until they are homogenous and reach atemperature of 148° C.

It is envisioned that the system 10 may use one or more heating/coolingdevices 46. The heating device causes the temperature of the mixture torise to at least 148° C. in order to provide sufficient energy andbinder mobility for complete system homogenization, pigment wetting, andcolor development. The heating devices 46, which form a part of themixing station are configured to melt the dry ingredients and form ahomogenous molten compound.

Rotations of the auger 42 force the material flow into the coolingstation where the material is cooled to between 121° C. and 135 ° C. Thematerial's melting and mixing temperatures can vary depending onformulation and end use. Low viscosity, high binder products such asspray materials and 40-mil materials might be processed at temperatureof 121° C. and extruded at temperature of between 93° C. and 107° C. Ahigh viscosity, molecularly robust product may be heated to atemperature of between 176° C. and 204° C. and extruded at temperatureof between 135° C. and 148° C.

The mixing station 12 comprises a pellet cutting member 50, whichreceives the molten homogenous compound from the conduit 40. The cuttingmember 50 may contain a plurality of cutting blades, which intercept themolten flow and cut it into individual pellets using rotating precisioncut dies. In one preferred embodiment, the apparatus 10 comprises dieswith six (6) to twelve (12), 4 mm diameter openings arranged in acircular pattern around the perimeter of an extrusion die. The cuttingmember 50 cuts the liquefied plastic and extrudes them into a water bathof the cooling station 14. The water bath can be in the form of a tube52 formed integrally with the cutter head of the cutting member 50. Thewater provides a means for transporting the pellets from the cutter headto a sifter (which may include a centrifuge) for separation of thepellets from the water, where the water is separated and re-circulatedback. The water also cools the pellets and causes solidification of thepellets. The solid pellets can be between 4 mm and 6.5 mm in size in theshape of small cylinders, fixed length cylinders that are now pellets,particles, or drops of solid, homogenous, thermoplastic road markingmaterial. In one exemplary embodiment, when the melted pavement markingmixture is cooled below 46° C. it solidifies and hardens.

As the material exits the extruder and die, it flows into a continuouslyflowing water stream that can be heated and cooled to improve pelletintegrity, which is entirely formulation dependent. The water'sthroughput rate, velocity, and temperature as well as the total water inthe system can vary and is designed as a function of the system's ratedproduction capacity per hour.

An extruder control unit 90 is operationally connected to the augerextruder assembly 32 via suitable cables 92; the control unit 90 forms apart of the extruder mixer assembly 32. The extruder control unit 90 isconfigured to control zone temperature, rotational speed of the auger42, as well as the feed rate of the raw materials into the auger mixerassembly 32. The control unit 90 is in operational communication withsensors 94 that measure screw torque, screw speed, energy consumption,zone temperature, flow rate, material temperature and system pressure.

The water is re-circulated through the system using a closed loopconduit 54. A circulating pump is mounted in the loop conduit 54 tofacilitate movement of water through the cooling section 14. The flow ofwater is controlled by a control unit 100, which provides temperaturecontrol and flow rate. The control unit 100 processes signals receivedfrom various sensors mounted in the cooling station 14 and issuescontrol command to the pump and the heating member(s) 46.

A sieve or sifter assembly 60 is mounted at the junction of the coolingstation 14 and the drying station 16. The sifter assembly 60 allowswater to drop by gravity, while the solid pellets 68 are carried onto afluidized bed or conveyor 70 of the drying station 16. The force ofwater flow propels the cut material upward through piping where thepelletizing apparatus separates the pellets from the water and depositsthem onto an air-fed fluidized bed 70 for drying. The bed is angledslightly away from the pellet source toward the pellet coating station18 so that the force of gravity can move the material through theprocess. As an alternative, the material can be dried using acentrifugal dryer, which eliminates the need for the fluidized bed andthe pellets would move via vibrating table directly into the pelletcoating station. Air flow moves through the bed surface via numeroussmall air holes, and the rate of flow is adjusted so that the force“floats” the material pieces, effectively making them weightless so thatthey move slowly down the angled bed and into the pellet coatingstation.

The fluidized bed 70 can be formed as a conveyor, which is exposed to aflow of drying air schematically illustrated by arrows 72 in FIG. 1. Thesolid pellets carried by the conveyor 70 are exposed to a continuousflow of dry air causing evaporation of any remaining liquid from thepellet surface. As the vapor 74 rises from the pellets 68, the pellets68 become dry even as they are transported to a rotating pellet coatingvessel 76.

The pellet coating barrel or vessel 76 is mounted below a coatingcontainer 78, which houses a pellet coating material. A weight loss loadcell 80 is operationally connected to the coating container 78 in orderto regulate delivery of the pellet-coating material to the pelletcoating vessel 76. The pellet coating material can be a member selectedfrom a group containing kaolin clay, calcium carbonate, calcined clay,micronized waxes and other anti-clumping materials or a combination ofmaterials.

The pellet coating station 18 is utilized to modify the surface of thepellets so that they will remain free flowing after packaging andstorage. The free flowing nature of the material is necessary for easeof use during application. The pelletized material is deposited into asmooth walled, rotating barrel 76 with an angled axis inclined towardthe pellet source leaving the fluidized bed 70 for vibratory table. Asthe material falls into the rotating barrel 76, the coating agent ismetered from the coating container into the barrel at a flow ratecontrolled by the control unit in the form of the weight loss cell 80.As an alternative, the pellets can be coated by suspending the pelletcoating as solution in the water used to cool and transport thematerial.

The coated pellets 82 are unloaded from the barrel 76 into a packagingand/or shipping container 84, which can be in the form of atransportable drum. In one exemplary embodiment, when the material inthe rotating barrel 76 reaches levels sufficient to overflow the barrel76, the surface treated particles “spill” into finished goods packagingor into another storage vessel that can be used to dispense the finishedproduct into packaging or various sizes or bulk storage. Finished goodspackaging can range in size from five-gallon containers holdingapproximately 22 kg of material to Gaylord boxes containingapproximately 907 kg-997 kg to super sacks containing up to 1587 kg tobulk storage devices that can hold up to 19958 kg. The bulk storagedevice can be used to ship material in bulk and stored in bulk bins atthe customer's location.

The road marking mix pellets packaged in the drums 84 are shipped to thesite, where road markings need to be applied. The pellets are meltedusing conventional equipment and then extruded directly onto the roadsurface. The solid pellets produced by the system of the presentinvention save time and energy during a road marking process. Thepellets are easily transported and deposited into the convention roadmarking machines, where they are melted, while retaining theirhomogenous characteristics.

The composition of the materials processed into pellets generallyfollows government specification set forth in AASHTO M249-09. Each stateor project could have special requirements or variations of thisspecification, but they usually reference this specification withchanges. The specification provides compositional requirements andmelt/flow characteristics. Things that could change are the Color Box orCIE color coordinates for yellow materials. Additionally, supplementalspecification LADOTD 1015.10 can be used. The pellets can differ insize, pigment, as well as refractive index depending on the type andratio of ingredients of the raw material mix.

The road marking mix may employ higher binder (25% or more), specialtyapplication (audible and audible inverted), and applied by spray, ribbonextrude, spray extrude, screed extrude application techniques.Regardless of material or application, it will still meet thecompositional requirements in the government specification M249-09.

The method of the present invention allows creation of a pavementmarking material that has substantially less dust because the finishedproduct is a solid, homogenous dust free product. The pavement markingcomposition produced by the method of the present invention ishomogenized during manufacturing, thereby producing compositionallyidentical particles. Having particles that are identical allows forincreased process control and monitoring. Theoretically, one particlecan be tested for composition and physical properties due to thehomogenous nature of the finished product. Smaller samples can be takenwith greater certainty of testing accuracy.

Since the method produces homogenous mixture during the mixing andmelting stages, each particle produced will be compositionallyidentical, which will yield more reliable and repeatable test results.The strict temperature control allows improved consistency of the finalproduct. Additionally, when compared to conventional processes using a“buffer” of raw materials added to ensure that the finished materialpasses independent laboratory testing for composition, the pelletsproduced in the instant system do not require the “buffer,” which leadsto significant cost reduction in raw materials and optimization of theformulation.

Because all materials are melted into the final product, raw materialscan be purchased and added as a liquid, solid, powder, or paste form.The pelletized material can be produced at lower temperatures (149°C.+/−4° C.) in comparison to the conventional block process (177°C.+/−4° C.). The production process does not require a “batching”process so there is no break or time loss between batches as seen in the“dry blend” or “block” processes. Material cooling after particleformation is accelerated by the lower initial temperature and fastercooling rate. The cooling rate is a function of surface area. The pelletprocess yields material with much higher surface area than the “block”process, resulting in more efficient cooling.

The pellets produced in accordance with the present invention havesuperior storage stability. The pellets or particles are in the samephysical form that is placed on the highway as an exterior, UV andweather resistant coating. Therefore, the pellets can withstand exposureto moisture, heat, humidity for longer periods than the current productson the market. Conventional “dry blend” products are produced in apowder form that will absorb moisture and become a solid compressedblock over a long storage time. Moisture content causes increased energyto vaporize the moisture and the increased energy and heat will alsocause color and physical property degradation. When the material becomescompressed the melt time, energy consumed, and labor requirement isgreatly increased. “Block” material can withstand moisture as well, butthe boxes that it is packaged in can get wet and become a nuisance andefficiency killer for crews. Generally, thermoplastic is considered tohave a one-year storage life when stored indoors, away from directcontact with water. The pellet materials produced according to thisinvention could see that longevity at least doubled.

It is envisioned that the pellets 82 can be used in conventional meltvessels and application operations, as well as “tankless” applicationoperations. In a “tank less” process, no material would be heated inmelt vessels or kettles. The pellets or particles would be addedmanually, pneumatically, or by other automatic or semi-automaticconveyance to a system of pipes and extruders capable of heating thematerial “on demand” and without any preheating.

Many changes and modifications can be made in the system of the presentinvention without departing from the spirit thereof. I, therefore, praythat my rights to the present invention be limited only by the appendedclaims.

I claim:
 1. A road marking composition comprising a binder mixturecomprising one or more member selected from the group consisting ofrosin resins, waxes, and plasticizers, and a filler mixture includingreflective elements, and wherein the rosin resins group is comprised ofmodified rosin resins and rosin esters.
 2. The composition of claim 1,further comprising a hydrocarbon resin.
 3. The composition of claim 1,wherein the binder mixture comprises between 8% and 16% by weight ofrosin resin with a melt point of between 95° and 110° C., between 0.01%and 3% by weight of wax with a melt point of between 95° and 115° C.,and a non-drying plasticizer in the amount of between 0.01% and 3% byweight.
 4. The composition of claim 1, wherein the modified rosin resinscomprise rosin acids, maleic anhydride, and fumaric acid, and whereinthe rosin acids comprise one or more member selected from the groupconsisting of abeitic acid, neoabeitic acid, dehydroabeitic acid,levopimaric acid, pimaric acid, palustric acid, isopimaric acid, andsandarocopimaric acid.
 5. The composition of claim 1, wherein the rosinesters are comprised of one or more derivative obtained from thereaction of one or more rosin acids and one or more alcohol from thegroup of alcohols consisting of methanol, triethylene glycol, glycerol,and pentaerythritol.
 6. The composition of claim 1, wherein the waxesare selected from the group consisting of vegetable waxes, petroleumderived waxes, and synthetic waxes.
 7. The composition of claim 6,wherein the vegetable waxes comprise mixtures of long-chain aliphatichydrocarbons containing esters of fatty acids and alcohols.
 8. Thecomposition of claim 7, wherein the fatty acids are comprised of one ormore member selected from the group consisting of ricinoleic acid, oleicacid, linoleic acid, linolenic acid, stearic acid, palmitic acid,dihydroxy stearic acid, myristic acid, myristoleic acid, palmitoleicacid, sapeinic acid, elaidic acid, vaccenic acid, alpha-linolenic acid,arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoicacid, caprylic acid, capric acid, lauric acid, arachidic acid, behenicacid, lignoceric acid, and cerotic acid.
 9. The composition of claim 7,wherein the alcohols are comprised of one or more member selected fromthe group consisting of glycerol, ethanol, methanol, pentaerythritol,iso-propanol, isopropyl alcohol, butanol, dihydroxy butanol, and analcohol having a varying long-chain aliphatic hydrocarbon base.
 10. Thecomposition of claim 6, wherein the petroleum derived waxes arecomprised of one or more member selected from the group consisting ofsaturated n-alkanes, iso-alkanes, napthenes, alkyl-substituted aromaticcompounds, and napthene-substituted aromatic compounds.
 11. Thecomposition of claim 6, wherein the synthetic waxes comprisepolyethylene waxes, Fischer-Tropsch waxes, chemically modified waxes,and amide modified waxes.
 12. The composition of claim 11, wherein thepolyethylene waxes comprise ultra-high-molecular-weight polyethylene,high-density polyethylene, cross-linked polyethylene, medium-densitypolyethylene, linear low-density polyethylene, low-density polyethylene,very-low-density polyethylene, and copolymers.
 13. The composition ofclaim 11, wherein the Fischer-Tropsch waxes comprise an agent having achemical formula of CnH(2n+2).
 14. The composition of claim 1, whereinthe chemically modified waxes comprise one or more member selected fromthe group consisting of a hydroxyl group, a carboxyl group, a salt, anester group, and an acid group.
 15. The composition of claim 1, whereinthe plasticizers are comprised of one or more member selected from thegroup consisting of vegetable oils, synthetic alkyd oils, and phalates.16. The composition of claim 15, wherein the vegetable oils comprisefatty acids selected from the group consisting of ricinoleic acid, oleicacid, linoleic acid, linolenic acid, stearic acid, palmitic acid,dihydroxy stearic acid, myristic acid, myristoleic acid, palmitoleicacid, sapeinic acid, elaidic acid, vaccenic acid, alpha-linolenic acid,arachidonic acid, eicosapentaenoic acid, erucic acid, docosahexaenoicacid, caprylic acid, capric acid, lauric acid, arachidic acid, behenicacid, lignoceric acid, and cerotic acid.
 17. The composition of claim15, wherein the phthalates are comprised of one or more member selectedfrom the group consisting of dimethyl phthalate, diethyl phthalate,diallyl phthalate, di-n-propyl phthalate, di-n-butyl phthalate,diisobutyl phthalate, butyl cyclohexyl phthalate, di-n-pentyl phthalate,dicyclohexyl phthalate, butyl benzyl phthalate, di-n-hexyl phthalate,diisohexyl phthalate, diisoheptyl phthalate, butyl decyl phthalate,butyl(2-ethylhexyl) phthalate, di(n-octyl) phthalate, diisooctylphthalate, n-octyl n-decyl phthalate, diisononly phthalate,di(2-prpoylheptyl) phthalate, diisodecyl phthalate, diundecyl phthalate,diisoundecyl phthalate, ditridecyl phthalate, and diisotridecylphthalate.
 18. The composition of claim 2, wherein the binder mixturecomprises between 10% to 15% by weight of hydrocarbon resin, between0.05% and 3% by weight of rosin resin, between 0.05% and 3% by weight ofwax, and 0.05% and 2% by weight of plasticizer.
 19. The composition ofclaim 2, wherein the hydrocarbon resin is one or more member selectedfrom the group consisting of C-5 aliphatic hydrocarbon resins, C-9aromatic hydrocarbon resins, and a mixture thereof.
 20. The compositionof claim 19, wherein the C5 aliphatic hydrocarbon resins comprisetrans-1,3-pentadiene, cis-1,3- pentadiene, 2-methyl-2-butene,dicyclopentadiene, cyclopentadiene, and cyclopentene.
 21. Thecomposition of claim 19, wherein the C9 aromatic hydrocarbon resinscomprise vinyltoluenes, dicyclopentadiene, indene, methylstyrene,styrene, and methylindenes.
 22. The composition of claim 1, wherein thefiller mixture comprises titanium dioxide in the amount of between 10%and 12% by weight, reflective elements in the amount of between 30% and40% by weight, and ground calcium carbonate in the amount of between 34%and 42% by weight.
 23. The composition of claim 1, wherein the fillermixture comprises titanium dioxide in the amount of between 0.5% and 3%by weight, reflective elements in the amount of between 30% and 40% byweight, a yellow pigment in the amount of between 0.25% and 1.25% byweight, an orange pigment in the amount of 0.05% to 0.25% by weight, anda sufficient amount of ground calcium carbonate to constitute 100% ofthe road marking composition when mixed with the binder mixture.
 24. Thecomposition of claim 1, wherein the binder mixture and the fillermixture are heated to a temperature of between 121° C. and 204° C. toform a homogenous viscous molten road marking composition.
 25. Thecomposition of claim 24, wherein the molten road marking composition iscooled to a temperature of between 93° C. and 148° C., extruded and cutinto individual solid pellets.
 26. The composition of claim 25, whereinindividual solid pellets of the road marking composition are coated withan anti-clumping agent.
 27. The composition of claim 26, wherein theanti-clumping agent comprises one or more member selected from the groupconsisting of kaolin clay, calcium carbonate, micronized waxes, and amixture thereof.
 28. A process of making road marking material,comprising the steps of: a. admixing a pre-determined quantity of abinder mixture comprising rosin resins, waxes, and plasticizers with afiller mixture comprising reflective elements; b. heating the bindermixture with the filler mixture, while mixing, into a homogenous viscousmolten composition; c. subjecting the molten composition to an extrusionprocess; d. cutting extruded molten composition into a plurality ofindividual pellets; e. cooling and drying the individual pellets; and f.applying an anti-clumping coating to the individual pellets.
 29. Themethod of claim 28, comprising a step of adding a pre-determinedquantity of hydrocarbon-based resin during the step of mixing the bindermixture with the filler mixture.
 30. The method of claim 28, wherein thebinder mixture comprises between 8% and 16% by weight of rosin resinwith a melt point of between 95° and 110° C., between 0.01% and 3% byweight of wax with a melt point of between 95° and 115° C., and anon-drying plasticizer in the amount of between 0.01% and 3% by weight.31. The method of claim 29, wherein the binder mixture comprises between10% to 15% by weight of hydrocarbon resin, between 0.05% and 3% byweight of rosin resin, between 0.05% and 3% by weight of wax, and 0.05%and 2% by weight of plasticizer.
 32. The method of claim 28, wherein thefiller mixture comprises titanium dioxide in the amount of between 10%and 12% by weight, reflective elements in the amount of between 30% and40% by weight, and ground calcium carbonate in the amount of between 34%and 42% by weight.
 33. The method of claim 28, wherein the fillermixture comprises titanium dioxide in the amount of between 0.5% and 3%by weight, reflective elements in the amount of between 30% and 40% byweight, a yellow pigment in the amount of between 0.25% and 1.25% byweight, an orange pigment in the amount of 0.05% to 0.25% by weight, anda sufficient amount of ground calcium carbonate to constitute 100% ofthe road marking composition when mixed with the binder mixture.
 34. Themethod of claim 28, wherein the modified rosin resins comprise rosinacids, maleic anhydride, and fumaric acid, and wherein the rosin acidscomprise one or more member selected from the group consisting ofabeitic acid, neoabeitic acid, dehydroabeitic acid, levopimaric acid,pimaric acid, palustric acid, isopimaric acid, and sandarocopimaricacid.
 35. The method of claim 28, wherein the rosin esters are comprisedof one or more derivative obtained from the reaction of one or morerosin acids and one or more alcohol from the group of alcoholsconsisting of methanol, triethylene glycol, glycerol, andpentaerythritol.
 36. The method of claim 28, wherein the waxes areselected from the group consisting of vegetable waxes, petroleum derivedwaxes, and synthetic waxes.
 37. The method of claim 36, wherein thevegetable waxes comprise mixtures of long-chain aliphatic hydrocarbonscontaining esters of fatty acids and alcohols.
 38. The method of claim37, wherein the fatty acids are comprised of one or more member selectedfrom the group consisting of ricinoleic acid, oleic acid, linoleic acid,linolenic acid, stearic acid, palmitic acid, dihydroxy stearic acid,myristic acid, myristoleic acid, palmitoleic acid, sapeinic acid,elaidic acid, vaccenic acid, alpha-linolenic acid, arachidonic acid,eicosapentaenoic acid, erucic acid, docosahexaenoic acid, caprylic acid,capric acid, lauric acid, arachidic acid, behenic acid, lignoceric acid,and cerotic acid.
 39. The method of claim 37, wherein the alcohols arecomprised of one or more member selected from the group consisting ofglycerol, ethanol, methanol, pentaerythritol, iso-propanol, isopropylalcohol, butanol, dihydroxy butanol, and an alcohol having a varyinglong-chain aliphatic hydrocarbon base.
 40. The method of claim 36,wherein the petroleum derived waxes are comprised of one or more memberselected from the group consisting of saturated n-alkanes, iso-alkanes,napthenes, alkyl-substituted aromatic compounds, andnapthene-substituted aromatic compounds.
 41. The method of claim 36,wherein the synthetic waxes comprise polyethylene waxes, Fischer-Tropschwaxes, chemically modified waxes, and amide modified waxes.
 42. Themethod of claim 41, wherein the polyethylene waxes compriseultra-high-molecular-weight polyethylene, high-density polyethylene,cross-linked polyethylene, medium-density polyethylene, linearlow-density polyethylene, low-density polyethylene, very-low-densitypolyethylene, and copolymers.
 43. The method of claim 41, wherein theFischer-Tropsch waxes comprise an agent having a chemical formula ofCnH(2n+2).
 44. The method of claim 28, wherein the chemically modifiedwaxes comprise one or more member selected from the group consisting ofa hydroxyl group, a carboxyl group, a salt, an ester group, and an acidgroup.
 45. The method of claim 28, wherein the plasticizers arecomprised of one or more member selected from the group consisting ofvegetable oils, synthetic alkyd oils, and phalates.
 46. The method ofclaim 45, wherein the vegetable oils comprise fatty acids selected fromthe group consisting of ricinoleic acid, oleic acid, linoleic acid,linolenic acid, stearic acid, palmitic acid, dihydroxy stearic acid,myristic acid, myristoleic acid, palmitoleic acid, sapeinic acid,elaidic acid, vaccenic acid, alpha-linolenic acid, arachidonic acid,eicosapentaenoic acid, erucic acid, docosahexaenoic acid, caprylic acid,capric acid, lauric acid, arachidic acid, behenic acid, lignoceric acid,and cerotic acid.
 47. The method of claim 45, wherein the phthalates arecomprised of one or more member selected from the group consisting ofdimethyl phthalate, diethyl phthalate, diallyl phthalate, di-n-propylphthalate, di-n-butyl phthalate, diisobutyl phthalate, butyl cyclohexylphthalate, di-n-pentyl phthalate, dicyclohexyl phthalate, butyl benzylphthalate, di-n-hexyl phthalate, diisohexyl phthalate, diisoheptylphthalate, butyl decyl phthalate, butyl(2-ethylhexyl) phthalate,di(n-octyl) phthalate, diisooctyl phthalate, n-octyl n-decyl phthalate,diisononly phthalate, di(2-prpoylheptyl) phthalate, diisodecylphthalate, diundecyl phthalate, diisoundecyl phthalate, ditridecylphthalate, and diisotridecyl phthalate.
 48. The method of claim 29,wherein the hydrocarbon resin is one or more member selected from thegroup consisting of C-5 aliphatic hydrocarbon resins, C-9 aromatichydrocarbon resins, and a mixture thereof.
 49. The method of claim 48,wherein the C5 aliphatic hydrocarbon resins comprisetrans-1,3-pentadiene, cis-1,3- pentadiene, 2-methyl-2-butene,dicyclopentadiene, cyclopentadiene, and cyclopentene.
 50. The method ofclaim 19, wherein the C9 aromatic hydrocarbon resins comprisevinyltoluenes, dicyclopentadiene, indene, methylstyrene, styrene, andmethylindenes.
 51. A composition comprising a road marking substanceobtained by the method of claim
 28. 52. A composition comprising a roadmarking substance obtained by the method of claim 29.